RNF183 ring finger protein 183
Information
- Symbol
- RNF183
- Type
- protein-coding
- Description
- ring finger protein 183
- Entrez Gene ID
- 138065
- Genome
- hg19
- Position
- chr9:116,059,734-116,062,045
- Genome
- hg38
- Position
- chr9:113,297,454-113,299,765
- HGNC
- HGNC:28721 HGNC
- Ensembl
- ENSG00000165188 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 1 | 0 |
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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28 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000441031.3 | hg38 | chr9 | 113,297,093 | 113,299,196 | 2,104 |
ENST00000478815.1 | hg38 | chr9 | 113,297,454 | 113,299,765 | 2,312 |
ENST00000297894.5 | hg38 | chr9 | 113,297,454 | 113,303,271 | 5,818 |
ENST00000489339.2 | hg38 | chr9 | 113,297,093 | 113,303,376 | 6,284 |
ENST00000416588.2 | hg38 | chr9 | 113,297,443 | 113,298,865 | 1,423 |
ENST00000441031.3 | hg19 | chr9 | 116,059,373 | 116,061,476 | 2,104 |
ENST00000489339.2 | hg19 | chr9 | 116,059,373 | 116,065,656 | 6,284 |
ENST00000416588.2 | hg19 | chr9 | 116,059,723 | 116,061,145 | 1,423 |
ENST00000478815.1 | hg19 | chr9 | 116,059,734 | 116,062,045 | 2,312 |
ENST00000297894.5 | hg19 | chr9 | 116,059,734 | 116,065,551 | 5,818 |
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